Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ancestral: G | Ambiguity code: R

Chromosome 14:60648862 (forward strand) | View in location tab


with COSMIC COSM698206 (G/C), COSM164343 (G/T), COSM1300718 (G/A) ; HGMD-PUBLIC CM041438

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Variation displays